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Volume 11, Number 1,March 2018 ISSN 1995-6673 JJBS Pages 81 - 85 Jordan Journal of Biological Sciences

Morphometric Relationships of the giuris (Hamilton, 1822) in the Gorai River using Multi-linear Dimensions

Md. Abul Kalam Azad, Md. Yeamin Hossain*, Dalia Khatun, Most. Farida Parvin, Fairuz Nawer, Obaidur Rahman and Md. Alomgir Hossen

Department of Fisheries, Faculty of Agriculture, University of Rajshahi, .

Received July 24, 2017; Revised September 14, 2017; Accepted September 26, 2017

Abstract

The present study illustrates the first complete and inclusive information of morphometric relationships, including Length- Weight Relationships (LWRs) and Length-Length Relationships (LLRs), using a total of 13 linear dimensions of Glossogobius giuris (Hamilton, 1822) in the Gorai River, southwestern (SW) Bangladesh. Also meristic characters, including various fin-rays of the tank goby, have been studied. In total, 229 specimens of G. giuris were collected occasionally from the Gorai River during March 2016 to February 2017 by a variety of local fishing gears (e.g., cast, gill, and square lift net). Fin rays and scales (including lateral line scale) were counted by a magnifying glass. Different morphometric lengths were measured to 0.01 cm, and whole Body Weight (BW) was estimated ± 0.01 g for each individual. The fin formula of G. giuris is: dorsal, D1. VI; D2. 8–11 (II–III/8–11); pectoral, P1. 17–22 (II–VI/14–19); pelvic, P2. 10–13 (II–III/8–10); anal, A. 7–12 (II–IV/5–8); and caudal, C. 16–21 (IV–VIII/12–13), correspondingly. In the present study, Total Length (TL) varied from 4.3 to 26.9 cm and BW ranged from 0.67 to 146.55g. All LWRs were highly significant (p < 0.0001) with r2 values ≥ 0.975. Based on r2 value, LWR by BW vs. TL, BW vs. SL and BW vs. PoAnL were good fitted models among 13 equations. The present study would be very valuable for recognition and stock assessment of tank goby in the Gorai River, SW Bangladesh and in adjoining ecosystems.

Keywords: Tank goby; Fin rays; Glossogobius giuris; Meristic; Morphometric.

1999; Hossen et al., 2016). Moreover, in fisheries 1. Introduction research, appraising the well-being of individuals as well as evaluating the life history and the morphological traits The tank goby Glossogobius giuris (Hamilton, 1822), of populations of different locality greatly rely on belonging to the family , is a benthopelagic; morphometric characters (King, 2007; Hossain, 2010; amphidromous species occurring in sea-, brackish- and Hossain et al., 2013). fresh-waters. It is the only species of diverse To the best of our knowledge, a few studies, including Glossogobius, found in Bangladesh, locally known as Bele morphometric and meristic characters, Length-Weight (Rahman, 2005), Bhaila in , Tank goby in , Relationships (LWRs), food and feeding habits, Goby in Philippine (Freose and Pauly, 2016). G. giuris reproduction and breeding performance, have been inhabits streams, canals, ditches and ponds. This goby fish conducted on this species from other habitats (Hossain et is broadly distributed in coastal and estuarine as well as al., 2009; Mollah et al., 2012; Islam and Mollah, 2013; fresh waters alongside the coasts of East Africa, the Red Hossain, 2014; Islam et al., 2014; Kaur and Rawal, 2015; Sea and the Indian subcontinent to (Freose and Qambrani et al., 2015; Hossain et al., 2016; Saha et al., Pauly, 2016). It is very rich in protein and micronutrients 2016); however, no sound studies on this issue, covering a and has high market value (Islam and Joadder, 2005; Islam large number of linear dimensions, have been conducted et al., 2014). This fish is one of the dominant species in the yet from the Gorai River. Therefore, the present study is Gorai River (SW Bangladesh); hence, it is an important designed to describe the morphometric and meristic capture species for small- and large- scale fishermen characteristics of G. giuris systematically using large (Costa et al., 1999; Hossain et al., 2009). number of specimens from small to larger sizes over a Studies on morphometric and meristic features can be study period of one year from the Gorai River (SW constructive tools for exact identification of any species Bangladesh). and its classification (Begenal and Tesch, 1978; Jayaram,

* Corresponding author. e-mail: [email protected]. 82 © 2018 Jordan Journal of Biological Sciences. All rights reserved - Volume 11, Number 1

2. Materials and Methods regression analysis (Hossain et al., 2006). Best/ good model for both LWRs and LLRs was selected based on the In the present study, a total of 229 individuals of G. highest value of determination r2. Total number of fin rays giuris (Figure 1) were collected occasionally from the and scales from different body parts (including the lateral Gorai (distributary of Ganges River) River (Latitude: 23° line) were counted by using magnifying glass. Statistical 32' N; Longitude: 89° 31' E), SW Bangladesh during analyses were performed using Graph Pad Prism 6.5 March 2016 to February 2017 from artisanal fishers. The software. All statistical analyses were considered samples were caught using various types of traditional significant at 5% (p < 0.05). fishing gears, i.e., cast net (mesh size ranges: 1.5 - 2.5 cm), gill net (mesh size ranges: 1.5–2.0 cm), and square lift net (mesh size: ~2.0 cm). The fresh samples (dead fish) were instantly chilled in ice on site and preserved with 10% buffered formalin after arrival in the laboratory. Total Body Weight (BW) of each individual was taken using a digital electric balance with 0.01 g accuracy and different linear dimensions, i.e., lengths (Table 1 and Fig. 2) Figure 1. A photo of Glossogobius giuris which was collected were estimated to the nearest 0.01 cm using digital slide from the Gorai River, southwestern Bangladesh calipers. The LWR was estimated using the equation: W= a× Lb, where W is the body weight (BW, g) and L is the 13 different lengths in cm. The regression parameters a and b were calculated by linear regression analyses based on natural logarithms: ln (W) = ln(a) + b ln(L). Moreover, 95% Confidence Limit (CL) of a and b and the co-efficient of determination (r2) were estimated. Extremes outliers were removed from the regression analyses according to Froese (2006). A t-test was used to confirm whether b values obtained in the linear regressions were significantly Figure 2. Showing the morphometric measurements of Glossogobius giuris in the Gorai River, southwestern Bangladesh different from the isometric (b = 3) value (Sokal and Rohlf 1987). A total of 12 LLRs were estimated by linear Table 1. Morphometric measurements of the Glossogobius giuris (Hamilton, 1822) (n = 229) captured from the Gorai River, southwestern Bangladesh

Min, minimum; Max, maximum; SD, standard deviation; CL, confidence limit for mean values; TL, total length; SL, standard length; BW, body weight; PrDL 1,1st Pre-dorsal length; PoDL 1,1st Post-dorsal length; PrDL 2, 2nd Pre-dorsal length; PoDL 2, 2nd Post-dorsal length; HL, Head length; OprL, Opercular length; PcL, Pectoral length; PvL, pelvic length; AnsL, anus length; PrAnL, pre-anal length; PoAnL, post-

Measurements Min (cm) Max (cm) Mean ± SD 95% CL %TL

TL (Total length) 4.3 26.9 12.803±5.893 12.036-13.571 SL (Standard length) 3.3 19.5 9.867±4.535 9.276-10.457 76.728 PrDL 1(1st Pre-dorsal length) 1.2 7.8 3.679±1.705 3.457-3.901 37.291 PoDL 1(1st Post-dorsal length) 1.5 10.1 4.810±2.226 4.520-5.099 37.401 PrDL 2(2nd Pre-dorsal length) 1.9 11.6 5.658±2.594 5.320-5.995 43.996 PoDL 2(2nd Post-dorsal length) 2.5 15.6 7.564±3.470 7.112-8.016 58.822 HL (Head length) 0.9 6.3 2.914±1.362 2.737-3.092 22.664 OprL (Opercular length) 0.8 6.2 2.781±1.372 2.602-2.959 21.625 PcL (Pectoral length) 0.9 6.3 2.964±1.410 2.781-3.148 23.051 PvL (Pelvic length) 1.1 6.4 3.110±1.449 2.922-3.299 24.188 AnsL(Anus length) 1.4 11.8 5.535±2.710 5.182-5.888 43.045 PrAnL(Pre-anal length) 1.9 12.3 6.000±2.766 5.640-6.360 46.658 BW (Body weight) 0.67* 146.55* 27.731±33.217 23.406-32.056 anal length; *, weight in g). © 2018 Jordan Journal of Biological Sciences. All rights reserved - Volume 11, Number 1 83

meristic measurements are presented in Table 1 and 2, 3. Results respectively. In the present study, TL was ranged from 4.3 to 26.9 cm (mean ± SD = 12.80±5.89) and the BW was The body of G. giuris is elongated and moderately varied from 0.67 to 146.55g (mean ± SD = compressed, mouth oblique with prominent lower jaw and 27.731±33.217). The standard length (76.73%) contains flattened head. The body color is brownish yellow with 5 the high percentage of TL (Table 1). to 6 dark and rounded spots on its sides. Dorsal, pectoral The regression parameters (a and b), with their 95% and caudal fins mottled with small spots where darkest confidence intervals for LWRs, coefficients of spots are found along the spine of second dorsal fin. Pelvic determination (r2) of G. giuris, are given in Table 2. All fins united but attached to the body only from their LWRs were highly significant (p < 0.0001) with r2 anterior part. The morphometric measurements of G. values ≥ 0.975. Based on r2 value, LWR by BW vs. TL, giuris are shown in Figure2. BW vs. SL and BW vs. PoAnL were good fitted models The fin formula of G. giuris is: dorsal, D1. VI; D2. 8– among the 13 equations. 11 (II–III/8–11); pectoral, P 1. 17–22 (II–VI/14–19); Also, the LLRs are presented in Table 3 and all LLRs 2 pelvic, P 2. 10–13 (II–III/8–10); anal, A. 7–12 (II–IV/5–8); were also highly correlated with r values ≥ 0.990. and caudal, C. 16–21 (IV–VIII/12–13), respectively. A According to r2 value, LLR by TL vs. SL; TL vs. PoDL 2; completed lateral line is present. There are about 32-33 TL vs. PrAnL and TL vs. PoAnL were good fitted models scales in lateral line and 5.5 scales above lateral line and among 12 equations. 6.5 scales below the lateral line. All morphometric and Table 2. Descriptive statistics and estimated parameters of the length-weight relationships of Glossogobius giuris (Hamilton, 1822) (n = 229) from the Gorai River, southwestern Bangladesh Equation Regression parameter 95% CL of a 95% CL of b r2 a b BW= a × TLb 0.0102 2.910 0.0096-0.0102 2.882-2.937 0.995 BW= a × SLb 0.0222 2.902 0.0209-0.0236 2.875-2.929 0.995 BW= a × PrDL 1b 0.4168 2.849 0.3974-0.4370 2.812-2.886 0.990 BW= a × PoDL 1b 0.1862 2.876 0.1773-0.1957 2.844-2.908 0.993 BW= a × PrDL 2b 0.1104 2.907 0.1046-0.1165 2.875-2.939 0.993 BW= a × PoDL 2b 0.0487 2.895 0.0460-0.0515 2.866-2.924 0.994 BW= a × HLb 0.8289 2.827 0.7797-0.8812 2.770-2.885 0.976 BW= a × OprLb 1.1287 2.672 1.0669-1.1941 2.617-2.726 0.975 BW= a × PcLb 0.8422 2.775 0.7977-0.8892 2.725-2.825 0.981 BW= a × PvLb 0.6699 2.853 0.6336-0.7082 2.804-2.903 0.983 BW= a × AnsLb 0.1747 2.687 0.1654-0.1846 2.654-2.720 0.991 BW= a × PrAnLb 0.0998 2.869 0.0950-0.1049 2.841-2.897 0.994 BW= a × PoAnLb 0.0529 2.877 0.0500-0.0558 2.849-2.905 0.995 n, sample size; a and b are regression parameters; CL, confidence intervals for mean values; r2, co-efficient of determination Table 3. The estimated parameters of the length-length relationships (Y = a +b × X) of Glossogobius giuris (n= 229) from the Gorai River, southwestern Bangladesh

Equation Regression parameters 95% CL of a 95% CL of b r2 a b TL = a + b× SL 0.0003 1.298 -0.0976 to 0.0982 1.289-1.307 0.997 TL = a + b×PrDL 1 0.1166 3.448 -0.0095 to 0.243 3.417-3.479 0.995 TL = a + b×PoDL 1 0.0947 2.642 -0.0231 to 0.2126 2.620-2.665 0.996 TL = a + b×PrDL 2 -0.0232 2.267 -0.1392 to 0.0927 2.249-2.86 0.996 TL = a + b×PoDL 2 -0.0217 1.696 -0.1249 to 0.0814 1.683-1.708 0.997 TL = a + b× HL 0.2509 4.307 0.0714-0.4305 4.251-4.363 0.990 TL = a + b×OprL 0.9208 4.273 0.7457-1.0959 4.217-4.330 0.990 TL = a + b×PcL 0.4735 4.160 0.2988-0.6483 4.106-4.213 0.991 TL = a + b×PvL 0.2190 4.046 0.0365 - 0.4015 3.993-4.0990 0.991 TL = a + b×AnsL 0.7912 2.170 0.6831-0.8994 2.153-2.188 0.996 TL = a + b×PrAnL 0.0415 2.127 -0.0612 to 0.1442 2.111-2.143 0.997 TL = a + b×PoAnL 0.0618 1.711 -0.0381 to 0.1616 1.698-1.723 0.997 SL, standard length; ; PrDL 1,1st Pre-dorsal length; PoDL 1,1st Post-dorsal length; PrDL 2, 2nd Pre-dorsal length; PoDL 2, 2nd Post-dorsal length; HL, Head length; OprL, Opercular length; PcL, Pectoral length; PvL, pelvic length; AnsL, anus length; PrAnL, pre-anal length; PoAnL, post-anal length; a, intercept; b, slope; CL, confidence limit for mean values; r2, co-efficient of determination.

84 © 2018 Jordan Journal of Biological Sciences. All rights reserved - Volume 11, Number 1

4. Discussion Acknowledgement

The present study illustrates the first complete The authors would like to extend their sincere information on morphometric (LWRs and LLRs) and appreciation to (i) TWAS for research grants (Ref: RGA meristic characteristics of G. giuris from the Gorai River, No. 14-028 RG/BIO/AS_1; UNESCO FR: 324028574), southwestern Bangladesh. In this study, a total of 229 (ii) BARC, PIU, NATP-2, Sub-project ID: 484 for individuals from small to larger body sizes were used; technical (usage of equipments) supports. The present however, it was not possible to collect G. giuris smaller study is part of the research for M. Phil degree of the than 4.3 cm TL, which can be attributed that the senior author M.A.K. Azad. fishermen failed to catch the smaller size or selectivity of fishing gears (Hossain et al., 2012; Hossain et al., 2016a, Conflict of Interest b). In the present study, the maximum length was found 26.9 cm TL, which is quite close to the study of Talwar The authors declare that there is no conflict of interest and Jhingran, 1991 (30 cm) but lower than the maximum regarding the publication of the present paper. recorded value of 50.0 cm SL (Eccles, 1992). The absence of maximum sizes of G. giuris in the Gorai River might be References due to either the absence of larger-sized individuals in the populations in the fishing grounds (Hossain et al., 2016c, Ahmed ZF, Hossain MY and Ohtomi J. 2012. Modeling the d; 2017 ) or fishermen did not go where the larger size growth of silver hatchet chela Chela cachius (Cyprinidae) from exist. Indeed, maximum length is a helpful fool to estimate the Old in Bangladesh using multiple functions. Zool Stud, 51: 336–344. the growth parameters (i.e., asymptotic length, growth coefficient), thereby important for fisheries resource Bagenal JB and Tesch FW. 1978. Methods for assessment of planning and management (Ahmed et al., 2012; Hossain, fish production in freshwaters. Blackwell Scientific publication, 2016b, 2017). Oxford, p.361. The allometric co-efficient (b) values of LWRs may Carlander KD. 1969. Handbook of freshwater fishery biology, vary between 2.0 and 4.0 (Carlander, 1969); however, Vol. 1. The Iowa State University Press, Ames, IA, p.752. values ranging from 2.5 to 3.5 are more common (Froese, Costa T, Begum A and Alam SMN. 1999. From exclusion to 2006). In the present study, most of the b values were collective ownership: A case study of user-group within the limit (2.67–2.91) indicating negative allometric representatives in fisheries management in Bangladesh. growth pattern for G. giuris in the Gorai River, SW Caritas and Department of Fisheries (DoF), Bangladesh. Bangladesh which was dissimilar with Hossain et al. Eccles DH.1992. FAO species identification sheets for fishery (2009) (b= 3.07-3.09). However, the b values may vary in purposes. Field guide to the freshwater fishes of . the same species due to the amalgamation of one or more Prepared and published with the support of the United Nations factors including variations of growth in different body Development Programme (project URT/87/016). FAO, Rome. parts, sex, physiology, preservation methods and p.145. differences in the observed length ranges of the specimens Froese R and Pauly D. (Eds.) 2016. Fish base 2016, World Wide collected (Tesch, 1971; Hossen et al., 2016; Hossain et al., Web electronic publication. Available at: http://www.fishbase.org 2015; 2017, Nawer et al., 2017), which were excluded (accessed on 24 November 2016). during the present study. In addition, all LLRs were highly Froese R. 2006. Cube law, condition factor and weight-length correlated, which is not in accordance with Hossain et al. relationships: History, meta-analysis and recommendations. J (2009). However, the present study found the best/good Appl Ichthyol, 22: 241–253. model among equations using a number of different Hossain MS, Roy A and Rahman ML. 2016. Food and feeding lengths based on coefficient of determination, which habit of Bele Glossogobius giuris (Hamilton and Buchannan, would be very effective for comparison with any future 1822) collected from Mithamain of Kishoreganj districts, studies. northeastern Bangladesh. Int J Fish Aquat Stud, 4: 84–88. st In the present study, 6 fin rays in 1 dorsal fin and 8–11 Hossain MS, Sultana N. 2014. Morphometric characters and nd in 2 dorsal fin, 17–22 pectoral fin rays, 10–12 rays in length- weight relationship of Bele, (Glossogobius giuris) from attached pelvic fin, 7–12 anal fin rays and 16–21 caudal Mithamoin Hair, Kissorgonj, Bangladesh. J Bangladesh Agril fin rays were observed, which was more or less similar Univ, 12: 389–395. with the studies done by Talwar and Jhingran (1991) and Hossain MS. 2014. Reproductive Characteristics of Bele, Rahman (2005). Besides, we found a total of 32-33 scales Glossogobius giuris from Mithamoin Haor, Kissorgonj, in lateral line, which is in agreement with Rahman (2005). Bangladesh. World J Fish & Marine Sci, 6: 537–543. In conclusion, these findings would be a helpful tool Hossain MY. 2010. Morphometric relationships of length-weight for taxonomists to recognize G. giuris and for fishery and length-length of four Cyprinid small indigenous fish species managers/ biologists to instigate the stock assessment of the from the (NW Bangladesh). Turk J Fish Aquat Sci, remaining stocks of this species in the Gorai River, SW 10: 131–134. Bangladesh and other subtropical countries. Also, these Hossain MY, Ahmed ZF, Leunda PM, Jasmine S, Oscoz J, Miranda results will impart an important baseline for future R and Ohtomi J. 2006. Condition, length-weight and length-length studies within the Gorai River and surrounding relationships of the Asian striped catfish Mystus vittatus (Bloch, ecosystems. 1794) (Siluriformes: Bagridae) in the Mathabhanga River, southwestern Bangladesh. J Appl Ichthyol, 22: 304–307. Hossain MY, Hossen MA, Khairun Y, Bahkali AH and Elgorban AM. 2016a. Length-weight relationships of Dermogenys pusilla © 2018 Jordan Journal of Biological Sciences. All rights reserved - Volume 11, Number 1 85

(Zenarchopteridae) and Labeo bata (Cyprinidae) in the Ganges Islam MR and Mollah MFA. 2013. Morphological observation River (NW Bangladesh). J Appl Ichthyol, 32: 744-746. and PG-induced breeding of Glossogobius giuris (hamilton 1822). Hossain MY, Hossen MA, Khatun D, Nawer F, Parvin MF, J Sci Technol, 11: 171-180. Rahman O and Hossain MA. 2017. Growth, condition, maturity Islam MS, Tuly DM, Hasnahena M, Bahadur P and Hassan MR. and mortality of the Gangetic Leaf fish Nandus nandus (Hamilton, 2014. Induced breeding of freshwater Goby, Glossogobius giuris 1822) in the Ganges River (Northwestern Bangladesh). Jordan J (Hamilton,1822) in the Captivity: A preliminary Study. J Fish Biol Sci, 10: 57-62. Aquat Sci, 9: 24-32. Hossain MY, Hossen MA, Pramanik MNU, Ahmed ZF, Hossain Jayaram KC. 1999. The Freshwater Fishes of the Indian MA and Islam MM. 2016b. Length–weight and length–length Region. Narendra Publishing House, Delhi. P.551. relationships of three Ambassid fishes from the Ganges River Kaur V and Rawal YK. 2015. Length-weight relationship in (NW Bangladesh). J Appl Ichthyol, : 1279-1281. 32 Glossogobius giuris (Ham.) from Sukhna Lake, Chandigarh. Int J Hossain MY, Naser SMA, Bahkali AH, Yahya K, Hossen MA Sci Res, 4: 2007-2009. and Elgorban AM. 2016c. Life history traits of the flying barb King M. 2007. Fisheries Biology, Assessment and Esomus danricus (Hamilton, 1822) (Cyprinidae) in the Ganges Management. 2nd edition, Oxford Press, London, p.382. River, Northwestern Bangladesh. Pak J Zool, 48: 399-408. Mollah MFA, Yeasmine S, Hossen MB and Ahammad AKS. Hossain MY. Ohtomi J. Ahmed ZF, Ibrahim AHM and Jasmine S. 2012. Landmark-based morphometric and meristic variations of 2009. Length-weight and morphometric relationships of the Tank Glossogobius giuris in three stocks. J Bangladesh Agril Univ, 10: goby Glossogobius giuris (Hamilton, 1822) (Perciformes: 375–384. Gobiidae) in the Ganges of Northwestern Bangladesh. Asian Fish Sci, 22: 961–969. Nawer F, Hossain MY, Hossen MA, Khatun D, Parvin MF, Ohtomi J and Islam MA. 2017. Morphometric relationships of the Hossain MY, Rahman MM, Abdallah EM and Ohtomi J. 2013. endangered Ticto barb Pethia ticto (Hamilton, 1822) in the Biometric relationships of the Pool barb Puntius sophore Ganges River (NW Bangladesh) through multi-linear dimensions. (Hamilton 1822) (Cyprinidae) from three major rivers of Jordan J Biol Sci, 10: 199-203. Bangladesh. Sains Malays, 22: 1571–1580. Qambrani GR, Soomro AN, Palh ZA, Baloch WA and Tabasum Hossain MY, Rahman MM, Bahkali AH, Yahya K, Arefin MS, S. 2015. Reproductive biology of Glossogobius giuris (Hamilton), Hossain MI, Elgorban AM, Hossen MA, Islam MM and Masood in Manchar Lake Sindh, Pakistan J Aquac Res Development 6: Z., 2016d. Temporal variations of sex ratio, length-weight 392. relationships and condition factor of Cabdio morar (Cyprinidae) in the Jamuna (Brahmaputra River distributary) River, Northern Rahman AKA, 2005. Freshwater Fishes of Bangladesh (Second Bangladesh. Pak J Zool, 48: 1099-107. edition). The Zoological Society of Bangladesh, Department of Zoology, University of Dhaka, Dhaka-1000, 394 pp. Hossain MY, Rahman MM, Fulanda B, Jewel MAS, Ahamed F and Ohtomi J. 2012. Length–weight and length–length Saha BK, Hassan MF and Saha A. 2016. Some aspects of biology relationships of five threatened fish species from the Jamuna of the bar-eyed Goby Glossogobius giuris (Hamilton 1822) (Brahmaputra River tributary) River, northern Bangladesh. J Appl (Perciformes: Gobiidae) from Netrakona. J Asiat Soc Bangladesh Ichthyol, 28: 275–277. Sci, 42: 95–106. Hossain MY, Sayed SRM, Rahman MM, Ali MM, Hossen MA, Sokal RR and Rohlf FJ. (Eds.) 1987. Introduction to Elgorban AM, Ahmed ZF and Ohtomi J. 2015d. Length-weight biostatistics, 2nd Edition, Freeman Publication, New York. relationships of nine fish species from the Tetulia River, southern P.887. Bangladesh. J Appl Ichthyol, 31: 967- 969. Talwar PK and Jhingran AG. 1991. Inland fishes of India and Hossen MA, Hossain MY, Pramanik MNU, Nawer F, Khatun D, adjacent countries. A.A. Balkema, Rotterdam, p.541. Parvin MF and Rahman MM. 2016. Morphological Characters of Tesch FW. 1971. Age and growth. In: Methods for assessment Botia lohachata. J Coast Life Med, 4: 689-692. of fish production in fresh waters (ed. W.E. Ricker). Blackwell Islam MN and Joadder MAR. 2005. Seasonal variation of the Scientific Publications, Oxford, pp.99–13. proximate composition of freshwater gobi, G. giuris (Hamilton) from the river Padma. Pak J Biol Sci, 8: 532–536.